Evidence map›Paper›PMID 33956058›Full record

ArticleBlood advances2021

SETBP1 overexpression acts in the place of class-defining mutations to drive FLT3-ITD-mutant AML.

Suruchi Pacharne, Oliver M Dovey, Jonathan L Cooper, Muxin Gu, Mathias J Friedrich, Sandeep S Rajan, Maxim Barenboim, Grace Collord, M S Vijayabaskar, Hannes Ponstingl and 8 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. The impact of SETBP1 mutations in neurological diseases and cancer.Genes to cells : devoted to molecular & cellular mechanisms · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 7 institutions in 2 countries.

Suruchi PacharneWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0003-2992-6854
Oliver M DoveyWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Jonathan L CooperWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Muxin GuWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0003-4376-795X
Mathias J FriedrichWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0003-3184-0283
Sandeep S RajanWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0003-0074-6729
Maxim BarenboimDepartment of Pediatrics and Children's Cancer Research Center, Klinikum Rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Grace CollordWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0003-1924-4411
M S VijayabaskarWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Hannes PonstinglWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0001-7573-1703
Etienne De BraekeleerWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0003-4659-023X
Ruben BautistaWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Milena MazanWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
Roland RadDepartment of Medicine II, Klinikum Rechts der Isar, Technische Universität München, Munich, Germany.
Konstantinos TzelepisWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0002-4865-7648
Penny WrightDepartment of Pathology, and.
Malgorzata GozdeckaWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
George S VassiliouWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.ORCID 0000-0003-4337-8022
Wellcome/MRC Cambridge Stem Cell Institute · GBWellcome Sanger Institute · GBGerman Cancer Research Center · DENational Health Service · GBThe Gurdon Institute · GBTUM Klinikum · DEUniversity of Cambridge · GB

Funding

Cancer Research UK 23015Cancer Research UK C22324/A23015Medical Research Council MC_PC_17230Wellcome Trust 210926/Z/18/Z
6 · The paper itself

Abstract

Advances in cancer genomics have revealed genomic classes of acute myeloid leukemia (AML) characterized by class-defining mutations, such as chimeric fusion genes or in genes such as NPM1, MLL, and CEBPA. These class-defining mutations frequently synergize with internal tandem duplications in FLT3 (FLT3-ITDs) to drive leukemogenesis. However, ∼20% of FLT3-ITD-positive AMLs bare no class-defining mutations, and mechanisms of leukemic transformation in these cases are unknown. To identify pathways that drive FLT3-ITD mutant AML in the absence of class-defining mutations, we performed an insertional mutagenesis (IM) screening in Flt3-ITD mice, using Sleeping Beauty transposons. All mice developed acute leukemia (predominantly AML) after a median of 73 days. Analysis of transposon insertions in 38 samples from Flt3-ITD/IM leukemic mice identified recurrent integrations at 22 loci, including Setbp1 (20/38), Ets1 (11/38), Ash1l (8/38), Notch1 (8/38), Erg (7/38), and Runx1 (5/38). Insertions at Setbp1 led exclusively to AML and activated a transcriptional program similar, but not identical, to those of NPM1-mutant and MLL-rearranged AMLs. Guide RNA targeting of Setbp1 was highly detrimental to Flt3ITD/+/Setbp1IM+, but not to Flt3ITD/+/Npm1cA/+, AMLs. Also, analysis of RNA-sequencing data from hundreds of human AMLs revealed that SETBP1 expression is significantly higher in FLT3-ITD AMLs lacking class-defining mutations. These findings propose that SETBP1 overexpression collaborates with FLT3-ITD to drive a subtype of human AML. To identify genetic vulnerabilities of these AMLs, we performed genome-wide CRISPR-Cas9 screening in Flt3ITD/+/Setbp1IM+ AMLs and identified potential therapeutic targets, including Kdm1a, Brd3, Ezh2, and Hmgcr. Our study gives new insights into epigenetic pathways that can drive AMLs lacking class-defining mutations and proposes therapeutic approaches against such cases.

Indexed as

Leukemia, Myeloid, AcuteAcute DiseaseAnimalsDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseMiceMutationNuclear ProteinsNucleophosminAsh1l protein, mouseDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseNPM1 protein, humanNpm1 protein, mouseNuclear ProteinsNucleophosmin

Identifiers

PMID33956058
PMCPMC8114559
OpenAlexW3158744925

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.